Reinforced polymeric articles

ABSTRACT

Polymeric article reinforced with a reinforcing component. The reinforcing component includes a composition made from at least one polymer and graphene sheets.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.13/234,654, entitled “Reinforced Polymeric Materials,” filed Sep. 16,2011, which is a continuation of International Application No.PCT/US10/27440, filed Mar. 16, 2010, which claims priority to, and thebenefit of U.S. Provisional Application No. 61/160,590, filed on Mar.16, 2009, entitled “Reinforced Polymeric Articles,” the disclosures ofeach of which are incorporated by reference herein in their entirety.

This application is also related to pending U.S. application Ser. No.13/234,602, entitled “Polymeric Fibers and Articles Made Therefrom,”filed on Sep. 16, 2011 and U.S. application Ser. No. 13/234,668,entitled “Tire Cords,” filed on Sep. 16, 2011, the disclosures of eachof which are incorporated by reference herein in their entirety.

FIELD OF THE INVENTION

The present invention relates to polymeric articles reinforced with areinforcing agent made from compositions comprising at least one polymerand graphene sheets.

BACKGROUND

The physical properties of polymeric fibers (which can include,depending on the polymeric material, high modulus, high strength, hightoughness, high stiffness, high fatigue resistance (including bendingand expansion/compression fatigue resistance), dimensional stability,abrasion resistance, shrinkage, thermal degradation stability, andchemical resistance, among other attributes) have enabled them to bewidely used to reinforce many polymeric articles, including mechanicalrubber goods, belts, membrane fabrics, hoses, diaphragms, and the like.Their light weight and ease of processing have allowed polymeric fibersto replace metals partially or wholly in many applications.

It would, however, be desirable to obtain polymeric fibers havingfurther improved properties, including one or more of modulus, strength,dimensional stability, fatigue resistance, impact resistance, andshrinkage.

Improved modulus and/or strength per unit weight could, for example,allow for the construction of lighter polymeric goods. Improved modulusand/or strength could also permit the replacement of metals (such assteel) or reduction of the amount of metal used in certain applications.For example, alternative warp and/or weft cord constructions could beused for some reinforcing applications.

For example, alternative warp and/or weft cord constructions in a beltcould be used to be decrease the reinforcement weight per unit area,which could offer goods (including mechanical rubber goods) such asbelts having lower operating and end-use costs. Bending resistance andwarp crimp requirements could be improved, improving the hysteresisand/or dynamic elongation properties of reinforcing agents andreinforced articles.

Increased impact resistance and shock absorbance of reinforcing agentsand reinforced articles could lower maintenance costs and end-useperformance. Increased thermal and/or electrical conductivity couldoffer more end-use possibilities for reinforced polymer goods, such asself-cleaning articles and applications where static dissipativity isimportant.

Thermal shrinkage and dimensional stability of reinforced polymer goods(including mechanical goods) (such as braided hoses, wrapped hoses,membranes, profiles, and diaphragms) could increase their durability(particularly under flexing) and useful lifetime. Control of shrinkageforces can be important when processing articles, particularly thosehaving complex shapes.

SUMMARY OF THE INVENTION

Disclosed and claimed herein are articles comprising at least onepolymeric component and at least one reinforcing component, wherein thereinforcing component includes a composition that has a polymer andgraphene sheets.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a plot of the storage modulus vs. temperature ofmonofilaments comprising poly(ethylene terephthalate) containing 0.25wt. % graphene sheets and of commercial PET monofilaments.

DETAILED DESCRIPTION

Articles described herein comprise at least one polymeric component andat least one reinforcing component. The reinforcing component includes acomposition that comprises at least one polymer and graphene sheets. Thereinforcing component can be in any suitable form, such as fibers,yarns, cords, fabrics, strips, tapes, plies, etc.

Fibers described herein comprise a composition including a polymer andgraphene sheets. The fibers can be in the form of polyamides,polyesters, acrylics, acetates, modacrylics, spandex, lyocells, and thelike. Such fibers (also referred to herein as filaments) can take on avariety of forms, including, staple fibers (also referred to as spunfibers), monofilaments, multifilaments, and the like. The fibers canhave a number of different average diameters. For example, in someembodiments the fibers can have a number average diameter of about 1 μmto about 1.5 mm or of about 15 μm to about 1.5 mm.

The fibers can be of any cross-sectional shape. For example, they canhave a circular or substantially circular cross-section, or havecross-sections that are, for example, oval, star-shaped, multilobal(including trilobal), square, rectangular, polygonal, irregular, etc.They can also be hollow in their entirety or in part and can have afoam-like structure. The fibers can be crimped, bent, twisted, woven orthe like.

Fibers can be in the form of a multicomponent (such as a bicomponent)composite structure (these are also referred to as conjugate fibers),including, for example, multilayered structures comprising two or moreconcentric and/or eccentric layers (including inner core and outersheath layers), a side-by-side structure, or the like. These can beobtained, for example, by extruding two or more polymers from the samespinneret.

In one embodiment, each of the components of the structures include aform of the composition. In another embodiment, at least one of thecomponents include a form of the composition and another of thecomponents include a material without the composition. For example,other components (such as layers) may comprise other polymericmaterials.

Examples of bicomponent structures include fibers comprising a polyestercore and a copolyester sheath, a polyester core and a polyethylenesheath, a polyester core and a polyamide sheath, a poly(ethylenenaphthalate) core and a sheath of another polyester, a polyamide coreand a copolyamide sheath, a polyamide core and a polyester sheath, apolypropylene core and a polyethylene sheath, and the like.

The fibers can be formed into fabrics that comprise at least one fiberof the present invention. The fibers can also be formed into yarns thatcomprise at least one fiber of the present invention and can optionallycomprise other fibers. The yarns can be in the form of filament yarns,spun yarns, and the like. The yarns can additionally be formed intocords that comprise at least one yarn and/or filament of the presentinvention. Fabrics may be formed from one or more fibers, cords, yarns,etc.

The fibers, yarns, and/or cords can be formed into fabrics havingenhanced tensile properties and strengths and tenacities. The fabricscan be woven fabrics, non-woven fabrics (including spunbonded, spunlaid,spun laced, etc. fabrics), knit fabrics, and the like and can includeadditional components such as, for example, fibers, yarns, and/or cordsother than those comprising polymer and graphene. The fibers can also beformed into microfiber fabrics.

The polymers can be of any suitable type, including thermoplastics,elastomers, non-melt-processable polymers, thermoset polymers, etc.Examples of polymers include, but are not limited to: polyamides,polyesters, polyolefins (such as polyethylene, ultrahigh molecularweight polyethylene, linear low density polyethylene (LLDPE), lowdensity polyethylene (LOPE), high density polyethylene, polypropylene,and olefin copolymers), cellulosic polymers, rayon, cellulose acetate,acrylics, poly(methyl methacrylate) and other acrylate polymers,poly(phenylene sulfide) (PPS), poly(acrylonitrile) andpoly(acrylonitrile) copolymers (such as copolymers with vinyl acetate,methyl acrylate, and/or methyl methacrylate), melamine polymers,polybenzimidazole (PBI), polyurethanes (including thermoplastics andthermosets), poly(p-phenylene-2,6-benzobisoxazole) (PBO), polyphenylenebenzobisthiazole,poly{2,6-diimidazo[4,5-b:4′,5′-e]pyridinylene-1,4-(2,5-dihydroxy)phenylene})(PIPD), liquid crystalline polyesters, aramids (such as those sold byDuPont under the trademarks Kevlar® and Nomex®, includingpoly(m-phenylene isophtalamide)s and poly(p-phenylene terephthalamide)s,and co-poly-(paraphenylene/3,4′-oxydiphenylene terephthalamide)), andpolymers derived from polyurethane and aliphatic polyethers (includingpolyether polyols such as poly(ethylene glycol), poly(propylene glycol),poly(tetramethylene ether) glycol (PTMEG), and the like)).

Other polymers include, for example, styrene/butadiene rubbers (SBR),styrene/ethylene/butadiene/styrene copolymers (SEBS), butyl rubbers,ethylene/propylene copolymers (EPR), ethylene/propylene/diene monomercopolymers (EPDM), polystyrene (including high impact polystyrene),poly(vinyl acetates), ethylene/vinyl acetate copolymers (EVA),poly(vinyl alcohols), ethylene/vinyl alcohol copolymers (EVOH),poly(vinyl butyral), acrylonitrile/butadiene/styrene (ABS),styrene/acrylonitrile polymers (SAN), styrene/maleic anhydride polymers,poly(ethylene oxide), poly(propylene oxide), poly(acrylonitrile),polycarbonates (PC), polyamides, polyesters, liquid crystalline polymers(LCPs), poly(lactic acid), poly(phenylene oxide) (PPO), PPO-polyamidealloys, polysulfones (PSU), polyether sulfones, polyurethanes,polyetherketone (PEK), polyetheretherketone (PEEK), polyimides,polyoxymethylene (POM) homo- and copolymers, polyetherimides,fluoropolymers (such as polytetrafluoroethylene (PTFE), fluorinatedethylene propylene polymers (FEP), poly(vinyl fluoride), andpoly(vinylidene fluoride)), poly(vinylidene chloride), poly(vinylchloride), and epoxy polymers.

The polymers can be elastomers such as, for example, polyurethanes,copolyetheresters, rubbers (including butyl rubbers and naturalrubbers), styrene/butadiene copolymers,styrene/ethylene/butadiene/styrene copolymer (SEBS), polyisoprene,ethylene/propylene copolymers (EPR), ethylene/propylene/diene monomercopolymers (EPDM), polysiloxanes, and polyethers (such as poly(ethyleneoxide), poly(propylene oxide), and their copolymers).

Preferred polymers include polyamides and polyesters (including, forexample thermoplastic and semicrystalline polyamides and polyesters),aramides, polyolefins, and rayons.

Examples of suitable polyamides include, but are not limited to,aliphatic polyamides (such as polyamide 4,6; polyamide 6,6; polyamide 6;polyamide 11; polyamide 12; polyamide 6,9; polyamide 6,10; polyamide6,12; polyamide 10,10; polyamide 10,12; and polyamide 12,12), alicyclicpolyamides, and aromatic polyamides (such as poly(m-xylylene adipamide)(polyamide MXD,6) and polyterephthalamides such as poly(dodecamethyleneterephthalamide) (polyamide 12,T), poly(decamethylene terephthalamide)(polyamide 10,T), poly(nonamethylene terephthalamide) (polyamide 9,T),the polyamide of hexamethylene terephthalamide and hexamethyleneadipamide, and the polyamide of hexamethyleneterephthalamide, and2-methylpentamethyleneterephthalamide) and copolymers of the foregoing.Preferred polyamides include polyamide 6,6; polyamide 6; and copolymersof polyamide 6 and polyamide 6,6. The polyamide 6,6 may have a relativeviscosity of at least about 65 when measured in 96% formic acid. Thepolyamide 6 may have a relative viscosity of at least about 85 whenmeasured in 96% formic acid.

Examples of suitable polyesters include, but are not limited to,semiaromatic polyesters, such as poly(butylene terephthalate) (PBT),poly(ethylene terephthalate) (PET), poly(1,3-propylene terephthalate)(PPT), poly(ethylene naphthalate) (PEN), and poly(cyclohexanedimethanolterephthalate) (PCT)), aliphatic polyesters (such as poly(lactic acid),and copolymers thereof. Preferred polyesters are PET, PPT, and PEN.Particularly preferred is PET. Polyesters can include copolyetheresters.Preferred polyesters have an intrinsic viscosity of at least about 0.8when measured in ortho-chlorophenol.

The graphene sheets are graphite sheets preferably having a surface areaof at least about 100 m²/g to about 2,630 m²/g. In some embodiments, thegraphene sheets primarily, almost completely, or completely comprisefully exfoliated single sheets of graphite (these are approximately 1 nmthick and are often referred to as “graphene”), while in otherembodiments, they can comprise partially exfoliated graphite sheets, inwhich two or more sheets of graphite have not been exfoliated from eachother. The graphene sheets can comprise mixtures of fully and partiallyexfoliated graphite sheets.

One method of obtaining graphene sheets is from graphite and/or graphiteoxide (also known as graphitic acid or graphene oxide). Graphite can betreated with oxidizing and intercalating agents and exfoliated. Graphitecan also be treated with intercalating agents and electrochemicallyoxidized and exfoliated. Graphene sheets can be formed by ultrasonicallyexfoliating suspensions of graphite and/or graphite oxide in a liquid.Exfoliated graphite oxide dispersions or suspensions can be subsequentlyreduced to graphene sheets. Graphene sheets can also be formed bymechanical treatment (such as grinding or milling) to exfoliate graphiteor graphite oxide (which would subsequently be reduced to graphenesheets).

Graphite oxide can be reduced to graphene by chemical reduction usinghydrogen gas or other reducing agents. Examples of useful chemicalreducing agents include, but are not limited to, hydrazines (such ashydrazine, N,N-dimethylhydrazine, etc.), sodium borohydride,hydroquinone, citric acid, etc. For example, a dispersion of exfoliatedgraphite oxide in a carrier (such as water, organic solvents, or amixture of solvents) can be made using any suitable method (such asultrasonication and/or mechanical grinding or milling) and reduced tographene sheets.

One method of exfoliation includes thermal exfoliation andultrasonication of suspensions. The graphite can be any suitable type,including natural, Kish, and synthetic/pyrolytic graphites and graphiticmaterials such as, for example, graphitic carbon fibers (including thosederived from polymers), and highly oriented pyrolytic graphite.

In one method of preparing graphene sheets, graphite is first oxidizedto graphite oxide, which is then thermally exfoliated to form highsurface area graphene sheets in the form of thermally exfoliatedgraphite oxide. Such a method is generally described in U.S. Patent Pub.No. 2007/0092432, entitled “Thermally Exfoliated Graphite Oxide” byPrud'Homme et al., the disclosure of which is incorporated herein byreference. The thusly formed thermally exfoliated graphite oxide maydisplay little or no signature corresponding to graphite or graphiteoxide in its X-ray diffraction pattern.

Graphite oxide may be produced by any method known in the art, such asby a process that involves oxidation of graphite using one or morechemical oxidizing agents and, optionally, intercalating agents such assulfuric acid. Examples of oxidizing agents include nitric acid, sodiumand potassium nitrates, perchlorates, hydrogen peroxide, sodium andpotassium permanganates, phosphorus pentoxide, bisulfites, and the like.Preferred oxidants include KClO₄; HNO₃ and KClO₃; KMnO₄ and/or NaMnO₄;KMnO₄ and NaNO₃; K₂S₂O₈ and P₂O₅ and KMnO₄; KMnO₄ and HNO₃; and HNO₃. Apreferred intercalation agent includes sulfuric acid. Graphite can alsobe treated with intercalating agents and electrochemically oxidized.

The graphene sheets preferably have an average aspect ratio of about 100to 100,000 (where “aspect ratio” is defined as the ratio of the longestdimension of the sheet to the shortest dimension of the sheet).

The graphene sheets preferably have a surface area of from about 100m²/g to about 2,630 m²/g, or more preferably of from about 200 m²/g toabout 2,630 m²/g, or yet more preferably of from about 300 m²/g to about2,630 m²/g, or even more preferably from about 350 m²/g to about 2,630m²/g, or still more preferably of from about 400 m²/g to about 2,630m²/g, or further more preferably of from about 500 m²/g to about 2,630m²/g. In another preferred embodiment, the surface area is about 300m²/g to about 1,100 m²/g. A single graphite sheet has a maximumcalculated surface area of 2,630 m²/g. The surface area includes allvalues and subvalues therebetween, especially including 400, 500, 600,700, 800, 900, 100, 110, 1,200, 1,300, 1,400, 1,500, 1,600, 1,700,1,800, 1,900, 2,000, 2,100, 2,200, 2,300, 2,400, 2,500, and 2,630 m²/g.

Surface area can be measured using either the nitrogen adsorption/BETmethod at 77 K or a methylene blue (MB) dye method in a liquid solution.The dye method is carried out as follows. A known amount of graphenesheets is added to a flask. At least 1.5 g of MB per gram of graphenesheets is then added to the flask. Ethanol is added to the flask and themixture is ultrasonicated for about fifteen minutes. The ethanol is thenevaporated and a known quantity of water is added to the flask tore-dissolve the free MB. The undissolved material is allowed to settle,preferably by centrifuging the sample. The concentration of MB insolution is determined using a UV-vis spectrophotometer by measuring theabsorption at λ_(max)=298 nm relative to that of standardconcentrations.

The difference between the amount of MB that was initially added and theamount present in solution as determined by UV-vis spectrophotometry isassumed to be the amount of MB that has been adsorbed onto the surfaceof the graphene sheets. The surface area of the graphene sheets is thencalculated using a value of 2.54 m² of surface covered per milligram ofMB adsorbed.

The graphene sheets preferably have a bulk density of from about 0.1kg/m³ to at least about 200 kg/m³. The bulk density includes all valuesand subvalues therebetween, especially including 0.5, 1, 5, 10, 15, 20,25, 30, 35, 50, 75, 100, 125, 150, and 175 kg/m³.

The graphene sheets can be functionalized with, for example,oxygen-containing functional groups (including, for example, hydroxyl,carboxyl, and epoxy groups) and typically have an overall carbon tooxygen molar ratio (C/O ratio), as determined by elemental analysis ofat least about 1:1, or more preferably, at least about 3:2. Examples ofcarbon to oxygen ratios include about 3:2 to about 85:15; about 3:2 toabout 20:1; about 3:2 to about 30:1; about 3:2 to about 40:1; about 3:2to about 60:1; about 3:2 to about 80:1; about 3:2 to about 100:1; about3:2 to about 200:1; about 3:2 to about 500:1; about 3:2 to about 1000:1;about 3:2 to greater than 1000:1; about 10:1 to about 30:1; about 80:1to about 100:1; about 20:1 to about 100:1; about 20:1 to about 500:1;about 20:1 to about 1000:1. In some embodiments of the invention, thecarbon to oxygen ratio is at least about 10:1, or at least about 20:1,or at least about 35:1, or at least about 50:1, or at least about 75:1,or at least about 100:1, or at least about 200:1, or at least about300:1, or at least about 400:1, or at least 500:1, or at least about750:1, or at least about 1000:1; or at least about 1500:1, or at leastabout 2000:1. The carbon to oxygen ratio also includes all values andsubvalues between these ranges.

The surface of the graphene sheets can be modified by the addition ofmolecules including hydrocarbons, and those containing neutral orcharged functional groups, such as oxygen-, nitrogen-, halogen-,sulfur-, carbon-containing functional groups. Examples of functionalgroups include hydroxyl groups, amine groups, ammonium groups,sulphates, sulphonates, epoxy groups, carboxylate and carboxylic acidgroups, esters, anhydrides, and the like. The modifying molecules may bebound to the surface of the graphene sheets covalently, ionically, viahydrogen bonding, electrostatically, via physical adsorption, and thelike.

The graphene sheets can contain atomic scale kinks due to the presenceof lattice defects in the honeycomb structure of the graphite basalplane. These kinks can be desirable to prevent the stacking of thesingle sheets back to graphite oxide and/or other graphite structuresunder the influence of van der Waals forces. Kinks may also be desirablefor adjusting the moduli of the sheets in the composite applicationswhere at low strains the kinks yield at low stress levels and thusprovide a gradually increasing modulus (75 to 250 GPa), and at highstrains moduli as high as 1 TPa may be attained. The kinks can also bedesirable for mechanical interlocking in the composite structures.

The compositions can optionally further include additional polymersand/or additional additives, including stabilizers (such as thermal,oxidative, and/or UV light resistant stabilizers), nucleating agents,colorants (such as pigments, dyes, and the like), other nanofillers(such as nanoclays), other carbon-based fillers (such as carbonnanotubes, carbon black, graphite, and the like), lusterants,delusterants (e.g., titanium dioxide), lubricants, dye-adhesionpromoters, and the like.

The compositions preferably include at least about 0.0001 wt % graphenesheets, based on the total weight of the graphene sheets and polymer.The graphene sheets can be present in at least about 0.005 wt %, in atleast about 0.001 wt %, in at least about 0.01 wt %, in at least about0.05 wt %, in at least about 0.1 wt %, in at least about 0.2 wt %, or inat least about 0.25 wt % (where all weight percentages are based on thetotal weight of the graphene sheets and polymer.

Preferred ranges in which the graphene sheets are present in thecompositions include from about 0.0001 wt % to about 3 wt %, from about0.001 wt % to about 3 wt %, from about 0.005 wt % to about 3 wt %, fromabout 0.01 wt % to about 3 wt %, from about 0.01 wt % to about 2 wt %,from about 0.025 wt % to about 2 wt %, from about 0.05 wt % to about 2wt %, from about 0.05 wt % to about 1 wt %, from about 0.05 wt % toabout 0.5 wt %, from about 0.1 wt % to about 1 wt %, from about 0.1 wt %to about 0.5 wt %, and from about 0.1 wt % to about 0.3 wt % (where allweight percentages are based on the total weight of the graphene sheetsand polymer).

If the polymer is melt processable, the compositions can be made priorto fiber formation using any suitable melt-blending method, includingusing a single or twin-screw extruder, a blender, a kneader, or aBanbury mixer. In one embodiment, the compositions are melt-mixed blendswherein the non-polymeric ingredients are well-dispersed in the polymermatrix, such that the blend forms a unified whole.

The compositions can also be formed by dry blending polymer and a masterbatch containing polymer and graphene sheets prior to melt spinning. Insuch a method, the master batch preferably comprises up to about 50 wt %graphene sheets, or more preferably from about 2 wt % to about 20 wt %graphene, based on the total weight of the master batch.

The compositions can also be made by combining graphene sheets (andoptionally, additional components) with monomers that are polymerized toform the polymer.

The fibers can be formed by any suitable method such as, for example,extrusion, melt spinning, solvent (wet) spinning, dry spinning, gelspinning, reaction spinning, electrospinning, and the like. For example,when spinning, suitable nozzles (such as spinnerets) may be selected toform monofilament or multifilament fibers.

When melt spinning, a quench zone can be used for the solidification ofthe filaments. Examples of quench zones include cross-flow, radial,horizontal, water bath, and other cooling systems. A quench delay zonethat may be heat or unheated can be used. Temperature control may bedone using any suitable medium, such as a liquid (e.g. water), a gas(e.g. air), and/or the like.

Filaments and/or yarns can be subjected to one or more drawing and/orrelaxation operations during and/or subsequent to the spinning process.Drawing and/or relaxation processes can be combined with the spinningprocesses (such as by using a spin draw process), or can be done usingseparate drawing equipment to pre-spun fibers in form of monofilament ormultifilament yarns. The drawing process can be done, for example, byusing different speed single or duo godets or rolls, with heating (hotdrawing), without heating (cold drawing), or both. The draw ratio can becontrolled by heating and/or annealing during the quench delay zone.Heating can be achieved using heated godets, one or more hot boxes, etc.Relaxation can be done with heating (hot drawing), without heating (colddrawing), or both.

The spinning speed, spinline tension, spinline temperature, number ofdrawing stages, draw ratio, relaxation ratio, speed ratios between eachrelaxation and drawing step, and other parameters can vary. Theparameters of the drawing and/or relaxation processes can be selectedaccording to the polymer or polymers used, the polymer structures,processability requirements, and/or desired physical and/or chemicalproperties of the fibers and/or filaments.

Spinning and/or drawing processes can affect one or more of the degreeof crystallization, crystallization rates, crystal structure and size,crystalline orientation, amorphous orientation, and the like. Filamentand yarn properties (such as tensile modulus and strength) may vary as afunction of spinning and/or drawing processes. In certain cases it ispossible that the functionalized graphene sheets increase orientationand crystallization of the polymer structure during the spinningprocesses.

A spin finish oil may optionally be applied to the filament afterquenching, but before any drawing and/or relaxation steps. A finish oilmay also be optionally applied to fibers before or during subsequentprocesses such as twisting, weaving, dipping, and the like.

The fibers can be electrically conductive, meaning that they may have aconductivity of at least about 10⁻⁶ S/m. In some embodiments, the fiberspreferably have a conductivity of about 10⁻⁶ S/m to about 10⁵ S/m, ormore preferably of about 10⁻⁵ S/m to about 10⁵ S/m. In otherembodiments, the fibers have a conductivity of at least about 100 S/m,or at least about 1000 S/m, or at least about 10⁴ S/m, or at least about10⁵ S/m, or at least about 10⁶ S/m.

The reinforcing component can be treated with an adhesive prior to beingincorporated into the article. Examples of adhesives include RFL(resorcinol formaldehyde latex) dips, cement, isocyanates, epoxies, andthe like.

Examples of the polymeric component include, but are not limited to,resins comprising one or more of rubbers, elastomers, polyurethanes,polyolefins (such as ethylene and including substituted polyolefins andcopolymers (random and block), such as styrene-isoprene-styrene andstyrene-butadiene-styrene copolymers), chloropolymers (such aspoly(vinyl chloride) (PVC)), fluoropolymers, etc. The resins maycomprise additional components, such as additives.

Example of rubbers used in the articles of the invention include, butare not limited to, natural rubber, butyl rubber, polybutadiene,stryene-butadiene rubber, isobutylene-isoprene rubber, chlorobutylrubber, bromobutyl rubber, neoprene, polyisoprene, chloroprene rubber,nitrile rubber, etc.

Examples of reinforced articles include, but are not limited to, belts(such as conveyor belts, transmission belts, timing belts, v-belts,power transmission belts, pump belts, antistatic belts, etc.),diaphragms and membrane fabrics (such as those used in diaphragms, airbrakes, roofing, and the like), hoses (such as automotive under-hoodhoses, high pressure hoses, and the like), air springs, textilearchitectural components, etc. The articles include manufactured rubbergoods. Examples of belts include, but are not limited to, belts for openor closed mining operations, belts for transporting luggage and cargo(as in airports, for example), belts used in factory production, beltsused in shopping check-out areas, belts used in construction, belts usedin power plant operations, man lifts, etc.

EXAMPLES Example 1

Graphene sheets are added to poly(ethylene terephthalate) (PET) by meltcompounding in an extruder to yield a PET composition comprising about0.25 weight percent graphene sheets. The PET composition is then solidphase polymerized at 215° C. to an IV of about 1 dL/g. The compositionis spun into monofilaments that are then post drawn to a draw ratio ofabout 4 to 5. After drawing, the filaments have a diameter of about 120microns. The storage modulus of the monofilaments is then measured as afunction of temperature using a dynamic mechanical analyzer (DMA). Theresults are given in Table 1 and in FIG. 1.

Comparative Example 1

The storage modulus of commercial PET monofilaments having an IV ofabout 0.6 to 0.8 dL/g and a diameter of about 250 microns is measuredusing a DMA. The commercial PET and the PET of Example 1 have similartenacities The results are given in Table 1 and FIG. 1.

TABLE 1 Comparative Example 1 Ex. 1 Storage  32° C. 17.7 8.83 modulus 52° C. 22.9 8.99 (GPa)  70° C. 21.8 9.13  90° C. 20.7 9.00 110° C. 19.07.85 130° C. 16.3 5.21 150° C. 14.0 3.34 170° C. 11.2 2.56 190° C. 9.822.49 210° C. 8.89 2.45

1-8. (canceled)
 9. An article comprising: a polymeric component; amultilobal or multilayered component having a first reinforcingcomponent and a second reinforcing component; wherein the firstreinforcing component and/or the second reinforcing component comprise acomposition having a polymer and individual sheets of graphene; andwherein the multilobal or multilayered component has a diameter of about120 μm to about 1.5 mm.
 10. The article of claim 9, wherein themultilayered component comprises the first reinforcing componentpositioned concentrically, eccentrically, or side-by-side relative tothe second reinforcing component.
 11. The article of claim 9, whereinthe polymer is one or more selected from the group consisting ofpolyamides, polyesters, polyolefins, aramids, cellulosic polymers, andrayon.
 12. The article of claim 11, wherein the polymer is a polyamide.13. The article of claim 12, wherein the polyamide is one or more ofpolyamide 6,6; polyamide 6; and polyamide 6,6/polyamide 6 copolymers.14. The article of claim 11, wherein the polymer is a polyester.
 15. Thearticle of claim 14, wherein the polyester is one or more ofpoly(ethylene terephthalate), poly(ethylene naphthalate), andpoly(ethylene terephthalate)/poly(ethylene naphthalate) copolymers. 16.The article of claim 11, wherein the polymer is an aramid.
 17. Thearticle of claim 11, wherein the polymer is rayon.
 18. The article ofclaim 9, wherein the graphene sheets comprise atomic scale kinks, andwherein the graphene sheets are interlocked via the atomic scale kinks.